US2009028904A1PendingUtilityA1

Novel cochleate formulations

Assignee: BIODELIVERY SCIENCES INTERNATIPriority: Jan 22, 1999Filed: Apr 23, 2008Published: Jan 29, 2009
Est. expiryJan 22, 2019(expired)· nominal 20-yr term from priority
A61P 37/06A61P 35/00A61P 31/10A61P 31/04A61P 9/10A61P 31/12A61P 29/00A61P 25/20A61P 23/00A61K 31/7048A61K 31/11A61K 31/20A61K 31/472A61K 31/496Y10S436/829Y10T428/2984A61K 31/07A61K 38/13A61K 9/1274A61K 31/713A61K 36/54A61K 31/704
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Claims

Abstract

A process for producing a small-sized, lipid-based cochleate. Cochleates are derived from liposomes which are suspended in an aqueous two-phase polymer solution, enabling the differential partitioning of polar molecule based-structures by phase separation. The liposome-containing two-phase polymer solution, treated with positively charged molecules such as Ca 2+ or Zn 2+ , forms a cochleate precipitate of a particle size less than one micron. The process may be used to produce cochleates containing biologically relevant molecules.

Claims

exact text as granted — not AI-modified
1 . A cochleate composition comprising a population of cochleates, wherein the cochleates comprise:
 a negatively charged first lipid   a divalent cation or higher valency cation and   an additional biologically relevant molecule,   
     wherein the mean particle size of the cochleates is less than one micron. 
   
   
       2 . The cochleate composition according to  claim 1 , wherein the biologically relevant molecule bears a charge. 
   
   
       3 . The cochleate composition according to  claim 2 , wherein the biologically relevant molecule is positively charged. 
   
   
       4 . The cochleate composition according to  claim 2 , wherein the biologically relevant molecule is negatively charged. 
   
   
       5 . The cochleate composition according to  claim 1 , wherein the biologically relevant molecule is amphiphilic. 
   
   
       6 . The cochleate composition according to  claim 1 , wherein the biologically relevant molecule is hydrophobic. 
   
   
       7 . The cochleate composition according to  claim 1 , wherein the biologically relevant molecule is at least one member selected from the group consisting of a drug, a polynucleotide, a polypeptide, an antigen, a nutrient and a flavor substance. 
   
   
       8 - 22 . (canceled) 
   
   
       23 . The cochleate composition according to  claim 1 , wherein the negatively charged lipid is comprised of phosphatidylserine. 
   
   
       24 . The cochleate composition according to  claim 1 , wherein the cochleates further comprise a minor amount of a second lipid. 
   
   
       25 . The cochleate composition according to  claim 24 , wherein the other lipid is a member selected from the group consisting of a zwitterionic lipid, a PEGylated lipid, a cationic lipid, or a polycationic lipid. 
   
   
       26 . The cochleate composition according to  claim 24 , wherein the second lipid comprises lipid capable of forming hydrogen bonds to the biologically relevant molecule. 
   
   
       27 . The cochleate composition according to  claim 1 , wherein the di- or higher-valent ions are metal ions. 
   
   
       28 . The cochleate composition according to  claim 27 , wherein the di- or higher-valent metal ions are selected from the group consisting of calcium, zinc, barium, and magnesium. 
   
   
       29 . A cochleate composition according to  claim 1  wherein the di- or higher-valent cation is a di or higher-valent cationic lipid. 
   
   
       30 - 63 . (canceled) 
   
   
       64 . A pharmaceutical composition comprising an effective amount of the cochleate composition of  claim 1  and a pharmaceutically acceptable carrier. 
   
   
       65 . (canceled) 
   
   
       66 . A method of treatment comprising administering to a human or animal host a pharmaceutically effective amount of the pharmaceutical composition according to  claim 64 . 
   
   
       67 . (canceled) 
   
   
       68 . The method of treatment according to  claim 66 , wherein the administration is by a mucosal or a systemic route. 
   
   
       69 . (canceled) 
   
   
       70 . The method of treatment according to  claim 66 , wherein the administration is a mucosal route selected from the group consisting of oral, intranasal, intraocular, intraanal, intravaginal, and intrapulmonary. 
   
   
       71 . (canceled) 
   
   
       72 . The method of treatment according to  claim 66 , wherein the administration is by a systemic route selected from the group consisting of intravenous, intramuscular, subcutaneous, transdermal and intradermal. 
   
   
       73 . The cochleate composition of  claim 7 , wherein the drug is an antifungal agent. 
   
   
       74 . The cochleate composition of  claim 7 , wherein the drug is a non-steriodal anti-inflammatory agent. 
   
   
       75 . The cochleate composition of  claim 7 , wherein the drug is an anticancer agent. 
   
   
       76 . The cochleate composition of  claim 7 , wherein the drug is selected from the group consisting of an antiviral, an anesthetic, or an anti-infectious agent, an immunosuppressant, a steroidal anti-inflammatory, a tranquilizer, and a vasodilatory agent. 
   
   
       77 . The cochleate composition of  claim 7 , wherein the drug is Amphotericin B. 
   
   
       78 . The cochleate composition of  claim 7 , wherein the drug is naproxen. 
   
   
       79 . The cochleate composition of  claim 7 , wherein the drug is Vitamin A acid. 
   
   
       80 . The cochleate composition of  claim 7 , wherein the drug is at least one member selected from the group consisting of acyclovir, adriamycin, carbamazepine, melphalan, nifedipine, indomethacin, naproxen, phenyloin, ergotamines, rapamycin, propanidid, propofol, alphadione, echinomycine, miconazole nitrate, teniposide, taxol, taxotere, nystatin, and rifampin. 
   
   
       81 . The cochleate composition of  claim 7 , wherein the drug is at least one member selected from the group consisting of estrogens, testosterones, steroids, cannabinoids, and vitamin A acid. 
   
   
       82 . The cochleate composition of  claim 7 , wherein the polynucleotide is a deoxyribonucletic acid (DNA) molecule 
   
   
       83 . The cochleate composition according to  claim 82 , wherein the DNA is transcribed to yield a ribonucleic acid. 
   
   
       84 . The cochleate composition of  claim 7 , wherein the polynucleotide is a ribonucleic acid (RNA) molecule. 
   
   
       85 . The cochleate composition according to  claim 84 , wherein the ribonucleic acid is translated to yield a biologically active polypeptide. 
   
   
       86 . A cochleate composition comprising a population of cochleates, wherein the cochleates comprise:
 a negatively charged lipid;   a divalent cation or higher valency cation; and, optionally,   an additional biologically relevant molecule,   
     wherein the mean particle size of the cochleates is less than one micron.

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